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The yeast tumor suppressor homologue Sro7p is required for targeting of the sodium pumping ATPase to the cell surface.

Wadskog, Ingrid (author)
Jönköping University,Gothenburg University,Göteborgs universitet,Institutionen för cell- och molekylärbiologi,Department of Cell and Molecular Biology,JTH, Kemiteknik
Forsmark, Annabelle, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för cell- och molekylärbiologi,Department of Cell and Molecular Biology
Rossi, Guendalina (author)
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Konopka, Catherine (author)
Oyen, Mattias (author)
Goksör, Mattias, 1975 (author)
Gothenburg University,Göteborgs universitet,Institutionen för fysik (GU),Department of Physics (GU)
Ronne, Hans (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Brennwald, Patrick (author)
Adler, Lennart, 1944 (author)
Gothenburg University,Göteborgs universitet,Institutionen för cell- och molekylärbiologi,Department of Cell and Molecular Biology
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 (creator_code:org_t)
2006
2006
English.
In: Molecular biology of the cell. - 1059-1524 .- 1939-4586. ; 17:12, s. 4988-5003
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The SRO7/SOP1 encoded tumor suppressor homologue of Saccharomyces cerevisiae is required for maintenance of ion homeostasis in cells exposed to NaCl stress. Here we show that the NaCl sensitivity of the sro7Delta mutant is due to defective sorting of Ena1p, the main sodium pump in yeast. On exposure of sro7Delta mutants to NaCl stress, Ena1p fails to be targeted to the cell surface, but is instead routed to the vacuole for degradation via the multivesicular endosome pathway. SRO7-deficient mutants accumulate post-Golgi vesicles at high salinity, in agreement with a previously described role for Sro7p in late exocytosis. However, Ena1p is not sorted into these post-Golgi vesicles, in contrast to what is observed for the vesicles that accumulate when exocytosis is blocked in sec6-4 mutants at high salinity. These observations imply that Sro7p has a previously unrecognized role for sorting of specific proteins into the exocytic pathway. Screening for multicopy suppressors identified RSN1, encoding a transmembrane protein of unknown function. Overexpression of RSN1 restores NaCl tolerance of sro7Delta mutants by retargeting Ena1p to the plasma membrane. We propose a model in which blocked exocytic sorting in sro7Delta mutants, gives rise to quality control-mediated routing of Ena1p to the vacuole.

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Keyword

Adenosine Triphosphatases
metabolism
Carrier Proteins
metabolism
Cation Transport Proteins
metabolism
Cell Membrane
drug effects
metabolism
Gene Expression
drug effects
Genes
Fungal
Golgi Apparatus
drug effects
Mutation
genetics
Protein Transport
drug effects
Recombinant Fusion Proteins
metabolism
Saccharomyces cerevisiae
cytology
drug effects
growth & development
ultrastructure
Saccharomyces cerevisiae Proteins
metabolism
Secretory Vesicles
drug effects
Sequence Homology
Sodium Chloride
pharmacology
Thermodynamics
Tumor Suppressor Proteins
metabolism
Vacuoles
metabolism
Adenosine Triphosphatases/*metabolism

Publication and Content Type

ref (subject category)
art (subject category)

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